Atlas FDA

Reader, nanoDot adapter, EU Model Number VINLADA003; radiation monitoring dosimeter used with the microSTAR readers

FDA device recall Z-2575-2023 · posted 2023-09-12 · Completed

Recall details

Recalling firm
Landauer
Reason for recall
LANDAUER received reports indicating that some nanoDots may potentially be outside of the specified range of +/-5.5% accuracy. Investigation of nanoDots indicated the presence of a potential non-conformance in the Optical Stimulated Luminescence (OSL) material that is beamed after exposure and emits fluorescence proportional to radiation exposure.
Action taken
Landauer disseminated an URGENT - Medical Device Recall notice to its consignees on 07/12/2023 by US mail and email. The notice explained the problem with the devices, potential risk, and requested the following: Discontinue use of the affected products, destroy used products, and return unused products.
Root cause
Under Investigation by firm
Status
Completed
Product code
IYE
Distribution
Worldwide
Date initiated
2023-07-12
Date posted
2023-09-12
Location
Glenwood, IL

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Related 510(k) clearances

RecordFirmDate
Medical Radiation Dosimetry System microSTARii (K192196)Landauer2019-12-27